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Clinical features of childhood-onset paroxysmal kinesigenic dyskinesia with PRRT2 gene mutations

Silveira-Moriyama, L; Gardiner, AR; Meyer, E; King, MD; Smith, M; Rakshi, K; Parker, A; ... Kurian, MA; + view all (2013) Clinical features of childhood-onset paroxysmal kinesigenic dyskinesia with PRRT2 gene mutations. DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY , 55 (4) pp. 327-334. 10.1111/dmcn.12056.

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Type: Article
Title: Clinical features of childhood-onset paroxysmal kinesigenic dyskinesia with PRRT2 gene mutations
DOI: 10.1111/dmcn.12056
Keywords: Science & Technology, Life Sciences & Biomedicine, Clinical Neurology, Pediatrics, Neurosciences & Neurology, HUMAN-CHROMOSOME 16, FAMILIAL INFANTILE CONVULSIONS, CHOREOATHETOSIS SYNDROME, HEMIPLEGIC MIGRAINE, MAJOR CAUSE, DISORDERS, LOCUS, IDENTIFICATION, LINKAGE, MAPS
UCL classification: UCL > Provost and Vice Provost Offices
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Clinical and Movement Neurosciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Department of Neuromuscular Diseases
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Pop Health Sciences > UCL GOS Institute of Child Health
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Pop Health Sciences > UCL GOS Institute of Child Health > ICH Developmental Neurosciences Prog
URI: http://discovery.ucl.ac.uk/id/eprint/1385333
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